Additional file 4 of Elevated HMGB1 promotes the malignant progression and contributes to cisplatin resistance of non-small cell lung cancer

Supplementary Material

Additional file 1 of Elevated HMGB1 promotes the malignant progression and contributes to cisplatin resistance of non-small cell lung cancer

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Additional file 3 of Elevated HMGB1 promotes the malignant progression and contributes to cisplatin resistance of non-small cell lung cancer

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Additional file 2 of Elevated HMGB1 promotes the malignant progression and contributes to cisplatin resistance of non-small cell lung cancer

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Additional file 6 of Elevated HMGB1 promotes the malignant progression and contributes to cisplatin resistance of non-small cell lung cancer

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Additional file 5 of Elevated HMGB1 promotes the malignant progression and contributes to cisplatin resistance of non-small cell lung cancer

Supplementary Material

Table_2_The Aging Features of Thyrotoxicosis Mice: Malnutrition, Immunosenescence and Lipotoxicity.xlsx

The problem of aging is mainly the increase of age-related diseases, and elderly patients have longer hospitalization and worse prognosis. Poorer nutritional status and immunosenescence may be predisposing and severe factors. The mechanism of the high incidence of diseases and poor prognosis behind aging is complex. Finding suitable aging models is of great significance to find strategies to prevent aging related events. In this study, the relationship between thyrotoxicosis and aging was investigated in mice. The results of routine blood tests and flow cytometry showed that immunosenescence occurred in thyrotoxicosis mice, which was characterized by a significant decrease in neutrophils, lymphocytes, CD4+/CD8+ and CD4+IFN-γ+ lymphocytes. Biochemical examination results showed that there were hypocholesterolemia, hypolipoproteinemia, and hyperlipidemia in thyrotoxicosis mice. Serum proteomics analysis showed that the downregulation of complement and coagulation proteins was another manifestation of declined immunity. Moreover, proteomics analysis showed that many downregulated proteins were related to homeostasis, mainly transport proteins. Their downregulation led to the disturbance of osmotic pressure, ion homeostasis, vitamin utilization, lipid transport, hyaluronic acid processing, and pH maintenance. Serum metabolomics analysis provided more detailed evidence of homeostasis disturbance, especially lipid metabolism disorder, including the downregulation of cholesterol, vitamin D, bile acids, docosanoids, and the upregulation of glucocorticoids, triglycerides, sphingolipids, and free fatty acids. The upregulated lipid metabolites were related to lipotoxicity, which might be one cause of immunosenescence and many aging related syndromes. This study provides evidence for the aging model of thyrotoxicosis mice, which can be used for exploring anti-aging drugs and strategies.</p

Organic Nanosheets of Imide-Linked Cathodes for High-Performance Aqueous Zinc-Ion Batteries

Organic electrodes have been identified as promising energy-storage materials for aqueous zinc-ion batteries (AZIBs). Small molecular materials have ideal redox properties, high specific capacity, and structural diversity, making them a category of cathode candidates for AZIBs. However, the instability and dissolution during the extraction and insertion of H+/Zn2+ limit their application of the long-cycle stability for AZIBs. Herein, a small-molecule nanosheet (NI-DAQ, ∼14 nm in thickness) with imide linkage is designed and synthesized by the condensation of anthraquinones and anhydrides. It not only inhibits the dissolution of monomer electrodes but also boosts the reactivity and conductivity of the whole molecule by the introduction of π-conjugated imide groups and extended aromatic planes. Therefore, the NI-DAQ electrode obtains a large initial capacity of 191.9 mA h g–1 at 50 mA g–1 and superior cyclability after 3000 cycles at 500 mA g–1 with a minor average capacity fading rate of 0.01% per cycle. Moreover, in situ Fourier transform infrared (FT-IR) and ex situ X-ray photoelectron spectroscopy (XPS) characterization techniques have been implemented to investigate the redox mechanism of CO units in AZIBs for the NI-DAQ electrode. Thus, a promising conductive molecule is developed and explored in this paper, which can provide insights into the application of organic materials in AZIBs

Boosted π‑Li Cation Effect in the Stabilized Small Organic Molecule Electrode via Hydrogen Bonding with MXene

The high solubility of the small organic molecule materials in organic electrolytes hinders their development in rechargeable batteries. Hence, this work designs an ultrarobust hydrogen-bonded organic–inorganic hybrid material: the small organic unit of the 1,3,6,8-tetrakis (p-benzoic acid) pyrene (TBAP) molecule connected with the hydroxylated Ti3C2Tx MXene through hydrogen bonds between the terminal groups of −COOH and −OH. The robust and elastic hydrogen bonds can empower the TBAP, despite being a low-molecule organic chemical, with unusually low solubility in organic electrolytes and thermal stability. The alkali-treated Ti3C2Tx MXene provides a hydroxyl-rich conductive network, and the small organic molecule of TBAP reduces the restacking of MXene layers. Therefore, the combination of these two materials complements each other well, and this organic–inorganic TBAP@D-Ti3C2Tx electrode delivers large reversible capacities and long cyclic life. Notably, with the assistance of the in situ FT–IR characterization of the electrode within the fully lithiated (0.005 V) and the delithiated (3.0 V) states, it is revealed that a powerful π-Li cation effect mainly governs the lithium-storage mechanism with the highly activated benzene ring and each C6 aromatic ring, which can reversibly accept six Li-ions to form a 1:1 Li/C complex

Table_4_The Aging Features of Thyrotoxicosis Mice: Malnutrition, Immunosenescence and Lipotoxicity.xlsx

The problem of aging is mainly the increase of age-related diseases, and elderly patients have longer hospitalization and worse prognosis. Poorer nutritional status and immunosenescence may be predisposing and severe factors. The mechanism of the high incidence of diseases and poor prognosis behind aging is complex. Finding suitable aging models is of great significance to find strategies to prevent aging related events. In this study, the relationship between thyrotoxicosis and aging was investigated in mice. The results of routine blood tests and flow cytometry showed that immunosenescence occurred in thyrotoxicosis mice, which was characterized by a significant decrease in neutrophils, lymphocytes, CD4+/CD8+ and CD4+IFN-γ+ lymphocytes. Biochemical examination results showed that there were hypocholesterolemia, hypolipoproteinemia, and hyperlipidemia in thyrotoxicosis mice. Serum proteomics analysis showed that the downregulation of complement and coagulation proteins was another manifestation of declined immunity. Moreover, proteomics analysis showed that many downregulated proteins were related to homeostasis, mainly transport proteins. Their downregulation led to the disturbance of osmotic pressure, ion homeostasis, vitamin utilization, lipid transport, hyaluronic acid processing, and pH maintenance. Serum metabolomics analysis provided more detailed evidence of homeostasis disturbance, especially lipid metabolism disorder, including the downregulation of cholesterol, vitamin D, bile acids, docosanoids, and the upregulation of glucocorticoids, triglycerides, sphingolipids, and free fatty acids. The upregulated lipid metabolites were related to lipotoxicity, which might be one cause of immunosenescence and many aging related syndromes. This study provides evidence for the aging model of thyrotoxicosis mice, which can be used for exploring anti-aging drugs and strategies.</p